Regioselective synthesis of 6-aryl-benzo[h][1,2,4]-triazolo[5,1-b]quinazoline-7,8-diones as potent antitumoral agents |
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Authors: | Liqiang wu Chong Zhang Weilin Li |
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Affiliation: | School of Pharmacy, Xinxiang Medical University, Xinxiang 453003, China |
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Abstract: | Three-component coupling of aldehyde, 2-hydroxy-1,4-naphthoquinone and 3-amino-1,2,4-triazole has been achieved using a catalytic amount of sulfamic acid under solvent free conditions to produce a novel series of 6-aryl-benzo[h][1,2,4]-triazolo[5,1-b]quinazoline-7,8-dione derivatives in good yields and with high regioselectivity. These compounds are found to exhibit potent antitumoral properties. |
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Keywords: | Sulfamic acid 2-Hydroxy-1,4-naphthoquinone Aldehydes Antitumor Solvent-free |
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